Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6850825

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:8,280

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 128 SVs from 24 studies. See in: genome view

Submitted genomic64,623,591-64,631,870

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6850825	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	64,623,591	64,631,870
nsv6850825	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	65,536,148	65,544,427

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18557977	deletion	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18557977	Submitted genomic		NC_000008.11:g.646 23591_64631870del	GRCh38 (hg38)		NC_000008.11	Chr8	64,623,591	64,631,870
nssv18557977	Remapped	Perfect	NC_000008.10:g.655 36148_65544427del	GRCh37.p13	First Pass	NC_000008.10	Chr8	65,536,148	65,544,427

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18557977	2.5e-05	7	275800

You are here: NCBI